ENST00000402696.9:c.1697C>G
MANE Select
|
ENSP00000385834.3:p.Pro566Arg
|
|
ENST00000402696.7:c.1697C>G
|
ENSP00000385834.3:p.Pro566Arg
|
|
ENST00000461695.1:c.428C>G
|
|
|
ENST00000467842.1:n.2691C>G
|
|
|
NM_001063.3:c.1697C>G
|
NP_001054.1:p.Pro566Arg
|
|
XM_011513100.1:c.1697C>G
|
XP_011511402.1:p.Pro566Arg
|
|
NM_001354703.1:c.1565C>G
|
NP_001341632.1:p.Pro522Arg
|
|
NM_001354704.1:c.1316C>G
|
NP_001341633.1:p.Pro439Arg
|
|
NM_001063.4:c.1697C>G
MANE Select
|
NP_001054.2:p.Pro566Arg
|
|
NM_001354703.2:c.1565C>G
|
NP_001341632.2:p.Pro522Arg
|
|
NM_001354704.2:c.1316C>G
|
NP_001341633.2:p.Pro439Arg
|
|